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. 2020 Dec 31;14:5757–5771. doi: 10.2147/DDDT.S278892

Table 1.

Applications of VAMS in Human (Clinical Trials)

Compound Sampling Technique, Matrix Analytical Technique Analytical Objective Reference
Caffeine Paraxanthine VAMS; Human blood UPLC-MS/MS To evaluate the potential of VAMS to eliminate the Hct effect and to evaluate the practical applicability and robustness of VAMS 49
Emixustat VAMS; Human whole blood LC-MS/MS To assess the potential for bridging PK data from plasma and blood collected via VAMS. 44
Fosfomycin VAMS; Human blood LC-MS/MS To perform an investigation into the extraction performance of the VAMS technique and to study the suitability of VAMS that would in a clinical PK study. 50
Vancomycin VAMS, DPS; human plasma LC-MS/MS To evaluate changes to extraction recovery across time for one analyte, the glycopeptide antibiotic vancomycin, in plasma using two dried microsampling formats, DPS and VAMS 51
Sulfur mustard VAMS; human plasma LC-ESI MS/MS To generate dried plasma samples not liable to the shipping constraints 52
Cathinone analogues VAMS; Human blood, urine and oral fluids LC-MS/MS To enhance and simplify drug concentration determination, in order to provide high- throughput reliable results and to establish methodology as a simple, feasible and reliable approach to determine the main synthetic cathinones in dried urine, plasma and oral fluid samples 53
Metoprolol, Midazolam, atorvastatin, tamoxifen, Amiodarone VAMS; Human blood LC-MS/MS To evaluate systematically extraction efficiency of drug molecules in VAMS dried blood samples and to assess the impact of blood Hct level. 54
Salbutamol VAMS; Human blood GC-MS To develop a simple, high throughput, quantitative assay for measurement of Salbutamol in micro-volume samples and to measure concentrations in the therapeutic and toxic range. 55
Miltefosine VAMS; Human whole blood LC-MS/MS To develop and validate an LC-MS/MS method for the quantification of Miltefosine in dried blood collected with the VAMS device and to compare performance with the previously published DBS method. 18
Atenolol, Lisinopril, Simvastatin Valsartan VAMS, DBS; Human blood LC–HRAM MS To compare the two-sampling methods DBS and VAMS and to demonstrate the potential utility of VAMS. 56
Praziquantel VAMS, DBS; Human whole blood LC-MS/MS To compare the quantification of the anthelmintic drug Praziquantel extracted from DBS and VAMS. 57
Oxycodone VAMS; Human whole blood and urine LC-MS/MS To explore VAMS suitability as an approach to urine sampling for anti-doping purposes and to compare the microsampling with classical sampling. 58
Protein analytes VAMS, DBS (FTA-DMPK cards GE Healthcare); Human whole blood NanoLC- SRM-MS To study quantitative method performance parameters such as the effect of blood hematocrit, matrix effects, response curve, repeatability and accuracy using concentration levels corresponding to the levels of medium to high abundance proteins in the blood. 15
Everolimus VAMS; Human blood LC-MS/MS To validate an LC-MS/MS method to quantify Everolimus using VAMS and to demonstrate its application and to investigate a range of Hct values. 59
Hydroxyurea DBS (Whatman 903 and FTA classic cards, GE Health), VAMS; Human blood LC-MS/MS To establish an analytically sensitive and specific method for the measurement of hydroxyurea in small volumes of whole blood obtained from pediatric patients and to achieve substantial technical improvement over existing methods in affording the routine analysis. 60
Voriconazole VAMS; Human blood LC-MS/MS To develop a sensitive assay for measuring Voriconazole and its major metabolites in a small volume of blood. 61
Adalimumab Ustekinumab Vedolizumab Tocilizumab Natalizumab Rituximab Infliximab VAMS; Human blood ELISA To measure drug levels of several therapeutic antibodies and to use an alternative (Mitra) microsampler to sampling capillary blood by traditional DBS on filter paper. 62